A Child with a Novel de novo Mutation in the Aristaless Domain of the Aristaless-Related Homeobox (ARX) Gene Presenting with Ambiguous Genitalia and Psychomotor Delay (English)
- New search for: Sirisena, Nirmala Dushyanthi
- New search for: McElreavey, Kenneth
- New search for: Bashamboo, Anu
- New search for: de Silva, K. Shamya H.
- New search for: Jayasekara, Rohan W.
- New search for: Dissanayake, Vajira H.W.
- New search for: Sirisena, Nirmala Dushyanthi
- New search for: McElreavey, Kenneth
- New search for: Bashamboo, Anu
- New search for: de Silva, K. Shamya H.
- New search for: Jayasekara, Rohan W.
- New search for: Dissanayake, Vajira H.W.
In:
Sexual Development
;
8
, 4
;
156-159
;
2014
- Article (Journal) / Electronic Resource
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Title:A Child with a Novel de novo Mutation in the Aristaless Domain of the Aristaless-Related Homeobox (ARX) Gene Presenting with Ambiguous Genitalia and Psychomotor Delay
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Contributors:Sirisena, Nirmala Dushyanthi ( author ) / McElreavey, Kenneth ( author ) / Bashamboo, Anu ( author ) / de Silva, K. Shamya H. ( author ) / Jayasekara, Rohan W. ( author ) / Dissanayake, Vajira H.W. ( author )
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Published in:Sexual Development ; 8, 4 ; 156-159
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Publisher:
- New search for: S. Karger AG
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Publication date:2014-08-01
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Size:4 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 8, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 139
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Congenital Adrenal Hyperplasia, Ovarian Failure and Ehlers-Danlos Syndrome due to a 6p DeletionMoysés-Oliveira, Mariana / Mancini, Tatiane I. / Takeno, Sylvia S. / Rodrigues, Andressa D.S. / Bachega, Tania A.S.S. / Bertola, Debora / Melaragno, Maria Isabel et al. | 2014
- 146
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No Mutations in the PSMC3IP Gene Identified in a Swedish Cohort of Women with Primary Ovarian InsufficiencyNorling / Hirschberg / Karlsson / Rodriguez-Wallberg / Iwarsson / Wedell / Barbaro et al. | 2014
- 151
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46,XY Disorder of Sex Development in a Sudanese Patient Caused by a Novel Mutation in the HSD17B3 GeneEllaithi, Mona / Werner, Ralf / Riepe, Felix G. / Krone, Nils / Kulle, Alexandra E. / Diab, Tayseer / Kamel, Alaa K. / Arlt, Wiebke / Holterhus, Paul-Martin / Sabir, Omyma et al. | 2014
- 156
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A Child with a Novel de novo Mutation in the Aristaless Domain of the Aristaless-Related Homeobox (ARX) Gene Presenting with Ambiguous Genitalia and Psychomotor DelaySirisena, Nirmala Dushyanthi / McElreavey, Kenneth / Bashamboo, Anu / de Silva, K. Shamya H. / Jayasekara, Rohan W. / Dissanayake, Vajira H.W. et al. | 2014
- 160
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A Lack of Association between Polymorphisms of Three Positional Candidate Genes (CLASP2, UBP1, and FBXL2) and Canine Disorder of Sexual Development (78,XX; SRY-Negative)Salamon, Sylwia / Nowacka-Woszuk, Joanna / Szczerbal, Izabela / Dzimira, Stanisław / Nizanski, Wojciech / Ochota, Malgorzata / Switonski, Marek et al. | 2014
- 166
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A Dual Role for SHH during Phallus Development in a MarsupialChew / Pask / Hickford / Shaw / Renfree et al. | 2014
- 178
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Gene Expression of Chicken Gonads Is Sex- and Side-SpecificScheider, Jessica / Afonso-Grunz, Fabian / Hoffmeier, Klaus / Horres, Ralf / Groher, Florian / Rycak, Lukas / Oehlmann, Jörg / Winter, Peter et al. | 2014
- X
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Front & Back Matter| 2014